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Upadacitinib in Patients with Psoriatic Arthritis and Inadequate Response to Biologics: 56-Week Data from the
Philip J Mease1,2, Apinya Lertratanakul3, Kim A Papp4
1Department of Rheumatology, Providence St. Joseph Health and University of Washington, Seattle, WA, USA. pmease@philipmease.com.
Upadacitinib maintained efficacy for psoriatic arthritis (PsA) patients over 56 weeks. This Janus kinase inhibitor showed no new safety concerns in patients with prior biologic treatment failure.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- Psoriatic arthritis (PsA) is a chronic inflammatory condition.
- Biologic therapies are common treatments for PsA.
- Some patients do not respond adequately or tolerate existing biologic therapies.
Purpose of the Study:
- To assess the 56-week efficacy and safety of upadacitinib in PsA patients.
- To evaluate upadacitinib in patients with an inadequate response or intolerance to biologic therapy.
Main Methods:
- Phase 3 SELECT-PsA 2 study involving 641 patients.
- Randomized, double-blind treatment with oral upadacitinib (15 or 30 mg daily) or placebo.
- Placebo group switched to upadacitinib at week 24; treatment duration was 56 weeks.
Main Results:
- Efficacy improvements (ACR20/50/70, PASI75/90/100, minimal disease activity) were maintained through 56 weeks.
- Patients switching from placebo to upadacitinib showed similar outcomes.
- Serious infection rates were 2.6 and 6.1 events/100 patient-years for 15 and 30 mg upadacitinib, respectively. Herpes zoster was more frequent with the 30 mg dose.
Conclusions:
- Upadacitinib demonstrated sustained efficacy in PsA patients over 56 weeks.
- No new significant safety signals were identified.
- Upadacitinib is a viable treatment option for PsA patients with prior biologic treatment failure.
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